Association between sodium‐glucose co‐transporter 2 inhibitors and risk of bullous pemphigoid in patients with type 2 diabetes: a nationwide population‐based cohort study

Background Certain anti‐diabetic agents have been linked to the development of bullous pemphigoid (BP). However, the relationship between BP and sodium‐glucose co‐transporter 2 inhibitors (SGLT2is) remains inconclusive. Objective To investigate the association between SGLT2i usage and BP. Methods Pa...

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Published inJournal of the European Academy of Dermatology and Venereology Vol. 36; no. 8; pp. 1318 - 1324
Main Authors Ma, S.H., Wu, C.Y., Lyu, Y.S., Chou, Y.J., Chang, Y.T.
Format Journal Article
LanguageEnglish
Published England 01.08.2022
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Summary:Background Certain anti‐diabetic agents have been linked to the development of bullous pemphigoid (BP). However, the relationship between BP and sodium‐glucose co‐transporter 2 inhibitors (SGLT2is) remains inconclusive. Objective To investigate the association between SGLT2i usage and BP. Methods Participants were recruited from the Taiwan National Health Insurance Database between 2007 and 2018. A total of 149 060 patients with diabetes receiving SGLT2i were matched 1 : 2 with diabetic patients without SGLT2i usage. Factors such as age, sex, duration of diabetes condition, DPP4i usage, insulin usage and selected comorbidities were included in the multivariate analysis. Results Compared with the control, the 2‐year‐cumulative incidence was significantly low in patients using SGLT2i after adjustment for competing mortality. Patients with diabetes receiving SGLT2i had a low risk [adjusted hazard ratio (HR) 0.56, 95% confidence interval (CI), 0.33–0.96] for BP after adjustment for potential confounders. Age (HR, 1.06), renal disease (HR, 1.79), cerebrovascular disease (HR, 3.23), epilepsy (HR, 3.07), DPP4i users (HR: 2.55) and insulin users (HR: 2.56) were significant risk factors for BP. Conclusions The risk of BP did not increase in patients receiving SGLT2i. Thus, SGLT2i could be a safe choice for patients with diabetes having additional risk factors or a history of BP.
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Linked Commentary
36
2022
This study was supported by the grants from the Ministry of Science and Technology, Taiwan, R.O.C. (MOST 108‐2314‐B‐075‐041‐MY3) and Taipei Veterans General Hospital (V110C‐021). The funding sources had no role in the design and conduct of the study; collection, management, analysis and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
The content of this manuscript has not been published entirely or in part, is not under consideration by another journal and will not be simultaneously submitted elsewhere.
https://doi.org/10.1111/jdv.18278
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J Eur Acad Dermatol Venereol
1162–1163.
Conflicts of interest
L. Mostaghimi & H. Noughani
None declared.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0926-9959
1468-3083
DOI:10.1111/jdv.18106